Canonical Allele Identifier: CA386302191

Gene: PAH

Linked Data

• MyVariant Identifiers: chr12:g.103271284T>C (hg19) ; chr12:g.102877506T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.102877506T>C , CM000674.2:g.102877506T>C	GRCh38
NC_000012.11:g.103271284T>C , CM000674.1:g.103271284T>C	GRCh37
NC_000012.10:g.101795414T>C	NCBI36
NG_008690.1:g.45097A>G
NG_008690.2:g.85905A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000553106.6:c.397A>G MANE Select	ENSP00000448059.1:p.Asn133Asp
ENST00000307000.7:c.382A>G	ENSP00000303500.2:p.Asn128Asp
ENST00000549111.5:n.493A>G
ENST00000550978.6:c.381A>G
ENST00000551337.5:c.397A>G	ENSP00000447620.1:p.Asn133Asp
ENST00000551988.5:n.486A>G
ENST00000553106.5:c.397A>G	ENSP00000448059.1:p.Asn133Asp
NM_000277.1:c.397A>G	NP_000268.1:p.Asn133Asp
XM_011538422.1:c.397A>G	XP_011536724.1:p.Asn133Asp
NM_000277.2:c.397A>G	NP_000268.1:p.Asn133Asp
NM_001354304.1:c.397A>G	NP_001341233.1:p.Asn133Asp
XM_017019370.2:c.397A>G	XP_016874859.1:p.Asn133Asp
NM_000277.3:c.397A>G MANE Select	NP_000268.1:p.Asn133Asp
NM_001354304.2:c.397A>G	NP_001341233.1:p.Asn133Asp